Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Reproductive hormones; Estrogens; Disease modifiers;
مقالات ISI ترجمه شده دیستروفی عضلانی FacioScapuloHumeral
مقالات ISI دیستروفی عضلانی FacioScapuloHumeral (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Audiometric follow-up data; Language level;
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Muscular dystrophy; Duchenne muscular dystrophy; Limb girdle muscular dystrophy; Facioscapulohumeral muscular dystrophy; Respiratory failure; Cardiomyopathy;
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; FSHD; D4Z4 macrosatellites; Southern blot; Anticipation;
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; FSHD1; Respiratory muscles; Pulmonary function;
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Ultrasound; Facioscapulohumeral muscular dystrophy; Skeletal muscle; Speckle tracking; Deformation imaging;
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Dermatomyositis; facioscapulohumeral muscular dystrophy; inclusion body myositis; mitochondrial cytopathy; muscular dystrophy; myopathy; myositis; myotonic dystrophy; polymyositis; statins
Specific muscle strength is reduced in facioscapulohumeral dystrophy: An MRI based musculoskeletal analysis
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Specific strength; Quantitative MRI; Musculoskeletal modeling; Intrinsic weakness;
Long-term results of Letournel scapulothoracic fusion in facioscapulohumeral muscular dystrophy: A retrospective study of eight cases
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Scapulothoracic fusion; Scapulothoracic arthrodesis; Letournel procedure; Facioscapulohumeral muscular dystrophy; Scapular winging;
Abnormal lipid metabolism in skeletal muscle tissue of patients with muscular dystrophy: In vitro, high-resolution NMR spectroscopy based observation in early phase of the disease
Keywords: دیستروفی عضلانی FacioScapuloHumeral; DMD; Duchenne muscular dystrophy; BMD; Becker muscular dystrophy; FSHD; Facioscapulohumeral muscular dystrophy; LGMD-2B; Limb girdle muscular dystrophy-2B; TG; Triglycerides; PL; Phospholipids; CHOL; Total cholesterol; TSP; [3-(trimethylsilyl) propionic-2
ReviewA complex interplay of genetic and epigenetic events leads to abnormal expression of the DUX4 gene in facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; FSHD1; FSHD2; DUX4; SMCHD1;
Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; D4Z4 repeat; Genotype–phenotype relationship; Gender difference
Facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Subtelomeric repeat; DNA methylation; SMCHD1; Epigenetics; DUX4;
Respiratory muscle dysfunction in facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Respiratory failure; Facioscapulohumeral muscular dystrophy; Pulmonary function tests; Mechanical ventilation; Neuromuscular respiratory dysfunction; AHI; apnea/hypopnea index; BMI; body mass index; ERV; expiratory reserve volume; FSHD; facioscapulohumera
Facioscapulohumeral Muscular Dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Muscular dystrophy; Facioscapulohumeral muscular dystrophy; D4Z4 deletion; DUX4; SMCHD1 mutation;
Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Infantile onset; Facioscapulohumeral muscular dystrophy; EcoRI fragment; Cardiac conductive defect; Restrictive ventilatory defect;
Dystrophie musculaire facio-scapulo-humérale de type 2
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Dystrophie musculaire facio-scapulo-humérale de type 2; Hypométhylation; DUX4; Ãpigenetique; Hérédité digénique; Facioscapulohumeral muscular dystrophy; Hypomethylation; DUX4; Epigenomics; Digenic transmission;
Relationships between clinical data and quantitative EMG findings in facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; myopathy; facioscapulohumeral muscular dystrophy; electromyography; motor unit potential; size indexmiopatia; dystrofia twarzowo-łopatkowo–ramieniowa; elektromiografia; potencjał czynnościowy jednostki ruchowej; wskaźnik wielkości
Value of muscle enzyme measurement in evaluating different neuromuscular diseases
Keywords: دیستروفی عضلانی FacioScapuloHumeral; DMD/BMD; Duchene/Becker muscular dystrophy; FSHD; facioscapulohumeral muscular dystrophy; LGMD; limb-girdle muscular dystrophy; PM; polymyositis; LSM; lipid storage myopathy; MND; motor neuron disease; SMA; spinal muscular atrophy; Muscle enzymes; Neuromu
Atypical onset in a series of 122 cases with FacioScapuloHumeral Muscular Dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; FacioScapuloHumeral Muscular Dystrophy; Atypical onset; Epilepsy; Myoglobinuria; Calpain;
Compound heterozygosity in a South African patient with Facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; FSHD; Compound heterozygote; Muscular dystrophy; Genotype-phenotype correlation;
Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Muscle computed tomography (CT); Muscle strength testing; D4Z4 fragment size;
Myopathies in the adult patient
Keywords: دیستروفی عضلانی FacioScapuloHumeral; dermatomyositis; facioscapulohumeral muscular dystrophy; inclusion body myositis; mitochondrial cytopathy; muscular dystrophy; myopathy; myositis; myotonic dystrophy; polymyositis; statins
Bilateral Coats’ response in a female patient leads to diagnosis of facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Coats’ disease; Optos fluorescein angiography; Retinal telangiectasia; Retinal exudation
Retinal vascular disease and the pathogenesis of facioscapulohumeral muscular dystrophy. A signalling message from Wnt?
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Myogenesis; Satellite cell; Wnt; Retina; Telangiectasis; Coats Disease;
Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; FRG1; Muscle; Z-disc; SarcomereFSHD, facioscapulohumeral muscular dystrophy; FRG1 FSHD, region gene 1; HSMM, human skeletal muscle myoblast; ICC, immunocytochemistry; MDSC, muscle-derived stem cell
Neuromuscular Electrical Stimulation Training: A Safe and Effective Treatment for Facioscapulohumeral Muscular Dystrophy Patients
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Isometric contraction; Quadriceps muscle; Rehabilitation; Shoulder; CK; creatine kinase; ES; effect size; FSHD; facioscapulohumeral muscular dystrophy; MMT; manual muscle test; MVIC; maximal voluntary isometric contraction; 6MWT; six-minute walk test; NME
Atteinte rétinienne et myopathies génétiques
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Rétinite pigmentaire; Dystrophie maculaire réticulaire; Maladie de Coats; Syndrome de Kearn et Sayre; MELAS; MIDD; Dystrophie musculaire facio-scapulo-humérale; Retinitis pigmentosa; Pattern retinal dystrophy; Coats disease; Kearn Sayre Syndrome; MELAS
Predictive values of motor unit potential analysis in limb muscles
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Biceps brachii; Facioscapulohumeral muscular dystrophy; Motor unit potential; Quantitative electromyography; Predictive values; Sensitivity; Specificity; Vastus lateralis
Sleep disordered breathing in facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Sleep; Sleepiness; Body mass index; Sleep disordered breathing; Polysomnography
Reduction of a 4q35-encoded nuclear envelope protein in muscle differentiation
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Nuclear envelope; Muscle differentiation; Facioscapulohumeral muscular dystrophy; Laminopathy
Periodic Salbutamol in Facioscapulohumeral Muscular Dystrophy: A Randomized Controlled Trial
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Clinical trial, Phase III; Facioscapulohumeral muscular dystrophy; Pharmacokinetics; Rehabilitation; SalbutamolECG, electrocardiogram; FSHD, facioscapulohumeral muscular dystrophy; MMT, manual muscle testing; MVIC, maximum voluntary isometric contractions
Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy - double trouble as an explanation for an atypical phenotype
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Atypical phenotype; Becker's muscular dystrophy; Dystrophin gene; Donor splice site mutation;
Facioscapulohumeral Muscular Dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; FSHD; facioscapulohumeral muscular dystrophy; muscular dystrophy; myostatin; chromosome 4;
The relationship between regional body composition and quantitative strength in facioscapulohumeral muscular dystrophy (FSHD)
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Body composition; DEXA; Dual-energy X-ray absorptiometry; Muscle strength; BMI; Lean tissue mass; Fat tissue mass
Chronic Pain in Persons With Myotonic Dystrophy and Facioscapulohumeral Dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Myotonic dystrophy; Pain; Rehabilitation;
DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; DUX4c; Myoblast
Sleep quality in Facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Sleep; Facioscapulohumeral muscular dystrophy; Sleepiness; Sleep quality; OSAS; Pittsburgh Sleep Quality Index; Epworth Sleepiness Scale;
Mobility assessment of patients with facioscapulohumeral dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Movement analysis; Motor capacity; Impairment severity; Shoulder range of motion; Gait; Step ascent; Squat
A role for epigenetics in hearing: Establishment and maintenance of auditory specific gene expression patterns
Keywords: دیستروفی عضلانی FacioScapuloHumeral; CpG; the DNA sequence “CG” where DNA methylation occurs; SINES; short interspersed transposable elements; LINES; long interspersed transposable elements; DNMT; DNA methyltransferase; siRNA; small interfering RNA; miRNA; Micro RNA; H; histone; HAT; his
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Pilot study; Folic acid; Methionine; DNA methylation
Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; Chromosome 4q35; Genetic diagnosis; Southern blotting; PCR; EcoRI fragment; D4Z4
Severe phenotype in infantile facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Muscular weakness; Infantile onset; Facioscapulohumeral muscular dystrophy
The genes encoding for D4Z4 binding proteins HMGB2, YY1, NCL, and MYOD1 are excluded as candidate genes for FSHD1B
Keywords: دیستروفی عضلانی FacioScapuloHumeral; Facioscapulohumeral muscular dystrophy; FSHD; D4Z4;
Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy
Keywords: دیستروفی عضلانی FacioScapuloHumeral; FSHD; Facioscapulohumeral muscular dystrophy; D4Z4; Mosaicism; Non-penetrance;